Astellas Pharma Associate CMC Regulatory Affairs Director in Northbrook, Illinois
Developing innovative therapies is one of the most challenging, most essential and personally rewarding fields in science. This is the most exciting time to be a part of Astellas, a company with a uniquely collaborative and patient-focused culture. There's something special about working at Astellas. It's reflected in our focus on the people we serve, the way we treat each other and the results we achieve together as a company. Astellas is announcing an Associate CMC Regulatory Affairs Director opportunity in Northbrook, IL.
Purpose & Scope:
This position plays a key global leadership role in the Regulatory Affairs department for the Chemistry, Manufacturing and Controls (CMC) aspects of regulatory documents and submissions. Responsible for multiple regulatory activities in collaboration with stakeholders (e.g., other RA functions, Pharmaceutical Technology, Quality Assurance, Business Partners). Responsible for developing global CMC regulatory strategy (e.g., CMC strategy/planning for NMEs), driving global CMC RA related activities and successfully executing regulatory strategies in collaboration with stakeholders. Responsible for supporting business critical interactions inside and outside of Astellas Regulatory Affairs on complex CMC issues and questions in collaboration with local and global stakeholders.
Essential Job Responsibilities:
Acts as a CMC regulatory lead and/or Deputy for highly complex projects/products and/or participates in non-product or overarching related activities.
May manage a small team or act as a mentor for one or more people.
Acts as CMC regulatory expert by global project teams/task forces and is accountable for recommending global CMC regulatory strategy. Works closely with other individuals/groups within Astellas global Regulatory Affairs and with local and global stakeholders to ensure consistency and to identify options for risk discussions.
Member of global project teams/task forces which require expert interpretation of applicable EMA/FDA/ICH/Global regulations to ensure CMC compliance within the organization. Sets direction for key operations and new initiatives in collaboration with local and global stakeholders.
Provides CMC regulatory expertise for New Product Planning and Licensing due diligence activities.
Manages the preparation and review of complex global registration packages to ensure effective data presentation and quality scientific data against applicable regulatory requirements. In collaboration with local and global stakeholders, determines the best way to present information in assigned regulatory submissions to maximize reviewability by global health authorities. Prepares and reviews summary tables of data from research and manufacturing reports, without direct supervision. Defines and implements regulatory strategies and priorities for; global registrations, supplemental submissions/variations,
This job description is intended to describe the general nature and level of work which may be performed by the person assigned to this position. This job
description is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of this position.
Employees holding this position may perform other job-related duties in the course of their performance of this position. Rev. 4.10.2015
response documents to health authority questions including Agency meeting planning and preparation, and global change control issues in collaboration with local and global stakeholders.
Oversees global submissions and ensures that the compilation and transmission of submissions are within the defined time schedules and meet established standards and SOPs. Reviews global regulatory submissions for consistency and quality across regions including detailed input on eCTD Module 3 documents for clinical trial and registration filings and DMFs.
Actively seeks out knowledge of overall corporate/global strategy and other general factors that affect the regulatory positions taken within the company, and with global health authorities, and incorporates this knowledge in interactions with others. Will also impact global strategy directly by participating in strategic planning in therapeutic area and with global stakeholders for chemistry, manufacturing and controls aspects.
Provides regulatory guidance for compendial issues, JP/EP/USP and other national compendial monographs, and monograph preparation.
Interacts with executive level on routine and serious matters; internally and externally to influence policy and strategy; with development partners; with global health authorities at review, management and senior staff, including negotiations on controversial areas. Established rapport with global health authorities that enables constructive exploratory discussions. Facilitator role in health authority meetings. Works on complex and diverse problems with decision making that has functional or corporate impact. Actions may have serious implications on operations, revenue, and/or credibility.
Reports to Director or Senior Director, Regulatory Affairs CMC.
BS in Chemistry or equivalent degree
10 years industry experience; pharmaceutical companies, CRO or academic with at least 6 years experience directly in Regulatory Affairs or in CMC regulatory or role with CMC regulatory submission responsibilities.
Experience with global regulatory aspects of CMC across multiple dosage forms involving undefined frameworks with technical complexity and broad scope.
Experience with process development, analytical characterization, process scale-up and/or regulatory registration of drug substances or drug products (including oral and parenteral dosage forms) is required.
Advanced interpersonal written and oral communication skills, as well as advanced collaborative skills with an ability to work both reactively and proactively in a timely manner in a dynamic fast-paced environment
Ability to manage complex projects by exercising independent decision making and analytical thinking skills
Knowledge/experience of EU, US and/or Japan regulations, guidelines and regulatory processes for NCEs, NBEs and product life cycle maintenance
Ability to work in cross-functional and international environment; detail- and goal-oriented, quality conscientious, and customer-focused
Ability to write and speak English fluently
Demonstrated track record for successful Health Authority interactions related to CMC submissions.
M.S. or Ph.D in Chemistry/Biochemistry, PharmD or equivalent degree with 6 years experience in CMC regulatory or role with CMC regulatory submission responsibilities
Experience managing direct report is preferred
Additional experience beyond small molecules, such as biologics, vaccines, cell/gene therapy or medical devices might be a preference.
Category Regulatory Affairs
Astellas is committed to equality of opportunity in all aspects of employment. EOE including Disability/Protected Veterans